Canonical Allele Identifier: CA2017437572

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562216_13562217delinsTA , CM000674.2:g.13562216_13562217delinsTA	GRCh38
NC_000012.11:g.13715150_13715151delinsTA , CM000674.1:g.13715150_13715151delinsTA	GRCh37
NC_000012.10:g.13606417_13606418delinsTA	NCBI36
NG_031854.1:g.422872_422873delinsTA
NG_031854.2:g.424796_424797delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*566_*567delinsTA MANE Select	ENSP00000477455.1:n.*566_*567delinsTA
ENST00000636207.1:n.54+21_54+22delinsTA
ENST00000637214.1:c.69+46386_69+46387delinsTA	ENSP00000489997.1:n.69+46386_69+46387delinsTA
ENST00000609686.3:c.*566_*567delinsTA	ENSP00000477455.1:n.*566_*567delinsTA
NM_000834.3:c.*566_*567delinsTA	NP_000825.2:n.*566_*567delinsTA
XM_005253351.2:c.*566_*567delinsTA	XP_005253408.1:n.*566_*567delinsTA
XM_011520628.1:c.*566_*567delinsTA	XP_011518930.1:n.*566_*567delinsTA
XM_011520629.1:c.*566_*567delinsTA	XP_011518931.1:n.*566_*567delinsTA
XM_011520630.1:c.*566_*567delinsTA	XP_011518932.1:n.*566_*567delinsTA
NM_000834.4:c.*566_*567delinsTA	NP_000825.2:n.*566_*567delinsTA
XM_005253351.3:c.*566_*567delinsTA	XP_005253408.1:n.*566_*567delinsTA
XM_011520628.2:c.*566_*567delinsTA	XP_011518930.1:n.*566_*567delinsTA
XM_011520629.2:c.*566_*567delinsTA	XP_011518931.1:n.*566_*567delinsTA
XM_017019219.2:c.*566_*567delinsTA	XP_016874708.1:n.*566_*567delinsTA
NM_000834.5:c.*566_*567delinsTA MANE Select	NP_000825.2:n.*566_*567delinsTA